The Needs of Patients with Psoriasis and Benefits of Apremilast in French Clinical Practice: Results from the Observational REALIZE Study.
Apremilast
PBI
Patient Benefit Index
Psoriasis
QOL
Quality of life
Real-world evidence
Treatment satisfaction
Journal
Dermatology and therapy
ISSN: 2193-8210
Titre abrégé: Dermatol Ther (Heidelb)
Pays: Switzerland
ID NLM: 101590450
Informations de publication
Date de publication:
Jun 2023
Jun 2023
Historique:
received:
10
03
2023
accepted:
28
04
2023
medline:
19
5
2023
pubmed:
19
5
2023
entrez:
19
5
2023
Statut:
ppublish
Résumé
Real-world data on the needs of patients with psoriasis and patient-perceived benefits of apremilast are limited. We report such data from France. The multicenter, observational REALIZE study was conducted in real-life clinical practice in France and enrolled patients with moderate-to-severe plaque psoriasis who had initiated apremilast per French reimbursement criteria in the 4 weeks preceding enrollment (September 2018-June 2020). Physician assessments and patient-reported outcomes (PROs) were collected at enrollment, 6 months, and 12 months. PROs included the Patient Benefit Index for skin diseases (PBI-S), Dermatology Life Quality Index (DLQI), and 9-item Treatment Satisfaction Questionnaire for Medication (TSQM-9). The primary outcome was PBI-S ≥ 1 (minimum clinically relevant benefit) at month 6. Of 379 enrolled patients who received ≥ 1 dose of apremilast, most [n = 270 (71.2%)] remained on apremilast at 6 months and over half [n = 200 (52.8%)] persisted at 12 months. Patients reported the following treatment goals as most important (≥ 70% reported goal as "very important" in the Patient Needs Questionnaire): get better skin quickly, regain disease control, be healed of skin alterations, and have confidence in the therapy. Most patients persisting on apremilast achieved a PBI-S ≥ 1 at months 6 and 12 (91.6% and 93.8%, respectively). Mean (SD) DLQI decreased from 11.75 (6.69) at enrollment to 5.17 (5.35) and 4.18 (4.39) at months 6 and 12, respectively. Most patients (72.3%) reported moderate-to-severe pruritus at enrollment and no/mild pruritus at months 6 and 12 (78.8% and 85.9%, respectively). Mean (SD) TSQM-9 Global Satisfaction scores were 68.4 (23.3) and 71.7 (21.5) at months 6 and 12, respectively. Apremilast was well tolerated; no new safety signals were identified. REALIZE provides insights regarding the needs of patients with psoriasis and the patient-perceived benefits of apremilast. Patients who persisted on apremilast reported improvements in quality of life, high treatment satisfaction, and clinically relevant benefits. NCT03757013. Psoriasis is a chronic disease and can have a large impact on patients’ quality of life. Patients often discontinue psoriasis treatments for a number of reasons, including side effects, ineffectiveness, and inconvenience. Apremilast (Otezla) is a twice-daily oral tablet for the treatment of moderate-to-severe plaque psoriasis. Data on the needs of patients with psoriasis and the patient-perceived benefits of psoriasis treatments, including apremilast, are limited. The REALIZE (Real Life Data for OTEZLA Evidence) study collected data from 379 patients with moderate-to-severe psoriasis receiving apremilast for up to 12 months in clinical practice across France. Patients completed questionnaires regarding their treatment goals, how well apremilast treatment met these goals, their quality of life, and their satisfaction with apremilast treatment. At the beginning of the study, patients reported getting better skin quickly, regaining control of their psoriasis, being healed of psoriatic lesions on their skin, and having confidence in their psoriasis treatment as their most important treatment goals. Over half of the patients continued apremilast for 12 months, with most reporting that apremilast successfully met their treatment needs. Patients also reported high satisfaction with apremilast and improved quality of life. The adverse events reported in the REALIZE study were similar to the known safety profile of apremilast. Our data show that apremilast is an effective, convenient, and well-tolerated treatment that improves the symptoms of psoriasis and meets patients’ needs and expectations.
Autres résumés
Type: plain-language-summary
(eng)
Psoriasis is a chronic disease and can have a large impact on patients’ quality of life. Patients often discontinue psoriasis treatments for a number of reasons, including side effects, ineffectiveness, and inconvenience. Apremilast (Otezla) is a twice-daily oral tablet for the treatment of moderate-to-severe plaque psoriasis. Data on the needs of patients with psoriasis and the patient-perceived benefits of psoriasis treatments, including apremilast, are limited. The REALIZE (Real Life Data for OTEZLA Evidence) study collected data from 379 patients with moderate-to-severe psoriasis receiving apremilast for up to 12 months in clinical practice across France. Patients completed questionnaires regarding their treatment goals, how well apremilast treatment met these goals, their quality of life, and their satisfaction with apremilast treatment. At the beginning of the study, patients reported getting better skin quickly, regaining control of their psoriasis, being healed of psoriatic lesions on their skin, and having confidence in their psoriasis treatment as their most important treatment goals. Over half of the patients continued apremilast for 12 months, with most reporting that apremilast successfully met their treatment needs. Patients also reported high satisfaction with apremilast and improved quality of life. The adverse events reported in the REALIZE study were similar to the known safety profile of apremilast. Our data show that apremilast is an effective, convenient, and well-tolerated treatment that improves the symptoms of psoriasis and meets patients’ needs and expectations.
Identifiants
pubmed: 37204608
doi: 10.1007/s13555-023-00933-z
pii: 10.1007/s13555-023-00933-z
pmc: PMC10196307
doi:
Banques de données
ClinicalTrials.gov
['NCT03757013']
Types de publication
Journal Article
Langues
eng
Pagination
1361-1376Commentaires et corrections
Type : ErratumIn
Informations de copyright
© 2023. The Author(s).
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